# Philips Medizin Systeme Boeblingen Gmbh – FDA Inspection, Sep 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/philips-medizin-systeme-boeblingen-gmbh/79bdbabe-0ee5-47d3-9fc9-a3d833d7e40e
Source feed: FDA_Inspections

> FDA inspection 682310 of Philips Medizin Systeme Boeblingen Gmbh, September 23, 2010. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 682310
- Company Name: Philips Medizin Systeme Boeblingen Gmbh
- Inspection Date: 2010-09-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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Company: https://www.keypedia.com/companies/philips-medizin-systeme-boeblingen-gmbh/736b3a4d-eb04-4b84-832d-87925302302a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7